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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1980229Erstellt: 26. Oktober 2026

Pyridine → alpha-Cyano-phenylacetic acid pentafluorophenyl ester

https://huagongshe.com/reaction/1980229

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktPentafluorophenolHCID 13041—
EduktPhosphorus pentachlorideHCID 24819—
Eduktalpha-Cyanobenzeneacetic acidHCID 26403—
LösungsmittelCarbon TetrachlorideHCID 5943—
LösungsmittelDichloromethaneHCID 6344—
Produktalpha-Cyano-phenylacetic acid pentafluorophenyl esterHCID 20402416—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

8 g. (0.05 moles) of α-cyano-phenylacetic acid are dissolved in 80 ml. of dichloromethane. 10.2 g. (0.05 moles) of phosphorus pentachloride are added and the mixture is stirred for two hours at the boiling point of dichloromethane. The solvent is distilled off and the residue is taken up in carbontetrachloride and the solution is added dropwise to 9.2 g. (0.05 moles) of pentafluorophenol and 4 ml. (0.05 moles) of pyridine-dissolved in 200 ml. of carbontetrachloride. The reaction mixture is cooled to 0° C. and the pyridine chlorohydrate is washed with 2n hydrochloride acid. The organic layer is washed twice with 40 ml. of water, dried over magnesium sulfate and evaporated. The α-cyano-phenylacetic acid-pentafluorophenyl ester is recrystallized from petrolether

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04508658
Quelldatensatzuspto-grants-1985_04
ORD IDord-b008978120024e89b3f15211d4f30f88
Quellennotizuspto-grants-1985_04